Intracranial embolism
diseaseOn this page
Summary
Intracranial embolism (MONDO:0006809) is a disease and 8 clinical trials. Top therapeutic interventions include egaptivon pegol. A subtype of ischemic stroke — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 8
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | intracranial embolism |
| Mondo ID | MONDO:0006809 |
| EFO | EFO:1000991 |
| MeSH | D020766 |
| DOID | DOID:4372 |
| ICD-11 | 816982857 |
| SNOMED CT | 75543006 |
| UMLS | C0752140 |
| MedGen | 155710 |
| Is cancer (heuristic) | no |
Disease family
This is a subtype of ischemic stroke. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › nervous system disorder › central nervous system disorder › brain disorder › cerebrovascular disorder › stroke disorder › ischemic stroke › intracranial embolism
Related subtypes (4): cerebral infarction, transient ischemic attack, brain stem infarction, pediatric arterial ischemic stroke
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 8.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 4 |
| PHASE3 | 2 |
| PHASE4 | 1 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00862160 | PHASE4 | UNKNOWN | Incidence of Acute Cerebrovascular Events Using Either Minimized or Standard Cardiopulmonary Bypass Circuit |
| NCT00336596 | PHASE3 | UNKNOWN | Ultrasound Enhanced Thrombolytic Therapy of Middle Cerebral Artery Occlusion |
| NCT03001960 | PHASE3 | UNKNOWN | Dual AntiPlatelet Therapies for Prevention of Periinterventional Embolic Events in TAVI |
| NCT00742612 | PHASE2 | TERMINATED | Effect of ARC1779 on Cerebral Microembolism in Patients Undergoing Carotid Endarterectomy |
| NCT01752946 | Not specified | UNKNOWN | A Registry Study of Shuxuening Injection Used in Hospitals in China |
| NCT02321917 | Not specified | COMPLETED | Rheoparin-coated Tubing System for Minimized Extracorporeal Circulation (MECC) |
| NCT02758964 | Not specified | COMPLETED | Evaluation of Cerebral Thrombembolism After TAVR |
| NCT02955004 | Not specified | COMPLETED | Electrical Cardioversion of Recent Onset Atrial Fibrillation - Silent Thromboembolic Events, Reverse Atrial Remodeling |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| EGAPTIVON PEGOL | 2 | 1 |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.